Collaborating with cross-functional teams to ensure timely and accurate data collection and ... Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ...
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Collaborating with cross-functional teams to ensure timely and accurate data collection and ... Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ...
Sr. Clinical Research Associate
Nevada, IA · On-site +1
... remote). * Actively participate in site feasibility assessments and site selection processes ... Utilize and maintain accurate study data in clinical systems, including Veeva Vault CTMS and CDMS.
Sr. Clinical Research Associate
Nevada, IA · On-site +1
... remote). * Actively participate in site feasibility assessments and site selection processes ... Utilize and maintain accurate study data in clinical systems, including Veeva Vault CTMS and CDMS.
Location: Remote Overall Job Summary: The Project Manager is the main point of contact for ... Coordinate with internal teams to query sites to submit incoming data and resolve data issues
New
Quick apply
Location: Remote Overall Job Summary: The Project Manager is the main point of contact for ... Coordinate with internal teams to query sites to submit incoming data and resolve data issues
New
Represent Pfizer Medical Affairs leadership with clinical/professional associations and/or ... Manage a significant volume of projects developed in a remote environment, while exhibiting the ...
Represent Pfizer Medical Affairs leadership with clinical/professional associations and/or ... Manage a significant volume of projects developed in a remote environment, while exhibiting the ...
... clinical/professional associations and/or societies, consistently demonstrating medical ... Manage a significant volume of projects developed in a remote environment, while exhibiting the ...
... clinical/professional associations and/or societies, consistently demonstrating medical ... Manage a significant volume of projects developed in a remote environment, while exhibiting the ...
Remote Clinical Data Abstractor information
See Ames, IA salary details
$13.87 - $16.10
8% of jobs
$18.04 is the 25th percentile. Wages below this are outliers.
$16.10 - $18.32
19% of jobs
$18.32 - $20.54
15% of jobs
The median wage is $21.83 / hr.
$20.54 - $22.77
14% of jobs
$22.77 - $24.99
12% of jobs
$24.99 - $27.21
6% of jobs
$28.60 is the 75th percentile. Wages above this are outliers.
$27.21 - $29.44
2% of jobs
$29.44 - $31.66
5% of jobs
$31.66 - $33.88
4% of jobs
$33.88 - $36.11
6% of jobs
$36.11 - $38.33
8% of jobs
$13
$24
$38
How much do remote clinical data abstractor jobs pay per hour?
As of Aug 17, 2026, the average hourly pay for remote clinical data abstractor in Ames, IA is $24.78, according to ZipRecruiter salary data. Most workers in this role earn between $18.12 and $31.25 per hour, depending on experience, location, and employer.
What are the key skills and qualifications needed to thrive as a remote clinical data abstractor?
To excel as a Remote Clinical Data Abstractor, you need a strong background in medical terminology, anatomy, and clinical documentation, often supported by experience in healthcare or a related degree. Familiarity with electronic health record (EHR) systems, data abstraction software, and certifications such as RHIA, RHIT, or CCS are highly valued. Attention to detail, self-motivation, and strong communication skills are essential soft skills in this remote role. These competencies ensure accurate extraction and management of clinical data, supporting compliance and quality improvement initiatives.
What are some common challenges faced by remote clinical data abstractors, and how can they be managed?
Remote Clinical Data Abstractors often encounter challenges such as managing large volumes of complex medical records, interpreting varied documentation styles, and maintaining accuracy under tight deadlines. Staying organized through effective time management and utilizing standardized abstraction guidelines can help mitigate these obstacles. Regular communication with clinical teams and ongoing training are also important for resolving ambiguities and staying updated on best practices. Adapting to a remote environment requires self-discipline, but with the right tools and support, most abstractors can excel and find satisfaction in the vital work they do.
What are popular job titles related to Remote Clinical Data Abstractor jobs in Ames, IA?
For Remote Clinical Data Abstractor jobs in Ames, IA, the most frequently searched job titles are:
What job categories do people searching Remote Clinical Data Abstractor jobs in Ames, IA look for?
The top searched job categories for Remote Clinical Data Abstractor jobs in Ames, IA are:
What cities near Ames, IA are hiring for Remote Clinical Data Abstractor jobs?
Cities near Ames, IA with the most Remote Clinical Data Abstractor job openings:
Full-time
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Re-posted yesterday
Job description
Senior CRA / CRA II - United States - Home Based
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.
What You Will Do:
You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement.
Key responsibilities include:
- Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
- Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
- Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
- Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
- Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.
Your Profile:
You will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others.
Required qualifications and experience:
- Bachelor's degree in a relevant scientific discipline or healthcare-related field
- Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
- Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
- Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
- Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
- Willingness to travel as required (approximately 60%)
#LI-LB1 #LI-REMOTE
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways
Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
Are you a current ICON Employee? Please click here to apply